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Water → HCID 19890426, 화합물

HRID 2073638
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HRID 2073638 반응식
[OH-].[Na+].O.[F:4][C:5]([F:26])([F:25])[CH:6]([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:7][CH2:8][O:9][C:10]1[CH:20]=[CH:19][C:13]([C:14]([O:16]CC)=[O:15])=[CH:12][CH:11]=1>CO>[F:4][C:5]([F:25])([F:26])[CH:6]([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:7][CH2:8][O:9][C:10]1[CH:20]=[CH:19][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962Water2회HCID 14798Sodium HydroxideHCID 19890431HCID 19890431, 화합물

생성물 1

HCID 19890426HCID 19890426, 화합물수율 90%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

In a round-bottomed flask, 0.27 g of sodium hydroxide and 1 ml of water were placed, 3 ml of methanol was added and then 0.7 g of ethyl p-(3-trifluoromethylheptyloxy)benzoate was added thereto, followed by 4 hours of reaction at 50° C. Then, water was added to the system, and methanol was distilled off, followed by addition of 6N-hydrochloric acid to recover a precipitated crystal. The crystal was dried in a desiccator to obtain 0.55 g of p-(3-trifluoromethylheptyloxy)benzoic acid ◯4 . (Yield: 90%).

후처리

  1. customfollowed by 4 hours of reaction at 50° C
  2. distillationwas distilled off
  3. additionfollowed by addition of 6N-hydrochloric acid
  4. customto recover a precipitated crystal
  5. customThe crystal was dried in a desiccator

출처 및 근거

ORD 기록
ord-b2eafc0542ea40e4a2519d91811c0e04
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04918213

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